ClinVar Miner

Submissions for variant NM_021098.3(CACNA1H):c.2010C>T (p.Gly670=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003056868 SCV003447147 benign Idiopathic generalized epilepsy; Hyperaldosteronism, familial, type IV 2022-09-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005010917 SCV005643218 uncertain significance Epilepsy, childhood absence, susceptibility to, 6; Hyperaldosteronism, familial, type IV 2024-02-12 criteria provided, single submitter clinical testing

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